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Reticulocyte hemoglobin content is the best indicator of iron deficiency in women with diffuse non-scarring hair loss.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Thorough hair examination is crucial for accurate diagnosis and treatment.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

A patient with Myotonic dystrophy type 1 had multiple tongue hemangiomas and was sensitive to anesthesia.

Splenic eumelanin in C57BL/6 mice is different from hair eumelanin.

PNH can occur in patients with SLE, so doctors should be aware of this.

Vitamin B12 deficiency can cause skin darkening and increased blood vessels, but treatment can improve symptoms.

The boy's symptoms suggest a possible new medical condition.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Two red-haired men with alopecia areata regrew black hair instead of red.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Many first-trimester pregnant women in Mysore have anemia and iron deficiency, needing better care and interventions.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

A woman's hair loss was treated successfully with iron supplements for her iron deficiency.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

RDW is a useful, cost-effective tool for diagnosing and monitoring various diseases.

People with normal hemoglobin but low ferritin experience more fatigue and certain symptoms like restless leg syndrome and dizziness.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

Iron supplements can restore normal hair color in cases of premature graying linked to iron deficiency.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Hair loss in women can improve with iron and vitamin supplements if caused by iron deficiency.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Monilethrix causes different levels of hair loss in family members.

Selenium deficiency caused symptoms in a child, which improved with selenium supplements.